Issue 0, 1967

The mechanism of the hydrolysis of glycofuranosides

Abstract

The mechanism of the acid-catalysed hydrolysis of a series of aldofuranosides has been investigated. These reactions are shown to involve glycosyl–oxygen fission and an initial rapid proton-transfer. The entropies of activation, which are all negative, are interpreted in terms of either a bimolecular displacement of MeOH or EtOH by H2O, or a mechanism involving ring-opening.

Article information

Article type
Paper

J. Chem. Soc. B, 1967, 185-189

The mechanism of the hydrolysis of glycofuranosides

B. Capon and D. Thacker, J. Chem. Soc. B, 1967, 185 DOI: 10.1039/J29670000185

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements